HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257524Generated: November 2, 2026
Methanol → Tert-butyl 3-bromo-5-(hydroxymethyl)benzoate
https://huagongshe.com/reaction/1257524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Tert-butyl methyl 5-bromoisophthalate | HCID 66896065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 3-bromo-5-(hydroxymethyl)benzoate | HCID 58096191 | 81.8% |
Reaction Steps
To a solution of tert-butyl methyl 5-bromoisophthalate (3.63 g, 11.5 mmol) in tetrahydrofuran (90 mL) at 0° C. was added portionwise sodium borohydride (1.53 g, 40.3 mmol). The mixture was stirred at 0° C. After 30 min, methanol (4.2 mL, 92.0 mmol) was added and the mixture was heated to 40° C. After 6 h, the mixture was cooled to ambient temperature and the mixture was quenched with methanol and concentrated. Ethyl acetate was added and the mixture was washed with brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes→50% hexanes/ethyl acetate) gave the title compound (2.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08461185B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-58805491a88f4125a5c9b26f9c6f4aec |
|---|
| Source note | uspto-grants-2013_06 |
|---|